In Situ Synthesis of 1D Mesoporous MnO@C Nanorods for High Performance Li-Ion Batteries

被引:22
作者
Li, Weiqin [1 ]
An, Cuihua [2 ]
Guo, Huinan [1 ]
Sun, Junli [1 ,3 ]
Wang, Mengying [1 ]
Li, Yunwei [1 ]
Jiao, Lifang [1 ]
Wang, Yijing [1 ]
机构
[1] Nankai Univ, Coll Chem, Minist Educ, Key Lab Adv Energy Mat Chem, Tianjin 300071, Peoples R China
[2] Tianjin Univ Technol, Sch Mat Sci & Engn, Tianjin Key Lab Adv Funct Porous Mat, Tianjin 300384, Peoples R China
[3] Chinese Peoples Armed Police Forces Acad, Langfang 065000, Hebei, Peoples R China
关键词
Lithium ion storage; MnO@C; Mesoporous material; 1D nanorods; Synergistic effect; METAL OXIDE NANOPARTICLES; ANODE MATERIALS; LITHIUM; CARBON; NANOWIRES; GRAPHENE; MICROSPHERES; STORAGE; DESIGN; GREEN;
D O I
10.1021/acssuschemeng.8b01782
中图分类号
O6 [化学];
学科分类号
0703 ;
摘要
Transition metal oxides have been regarded as the most potential anode material for lithium-ion batteries (LIBs), because of their high theoretical capacity, abundant resource, and low cost. Nevertheless, poor conductivity and large volumetric expansion during the charge-discharge processes make it difficult for LIBs application. In this work, we have adopted an in situ carbon coating method to synthesize 1D mesoporous MnO@C nanorods, which effectively work out the above problems of LIBs. Meanwhile, the MnO@C-3 (the mixture is 40 mL of H2O in solvothermal reaction) anode exhibits excellent rate capability with the capacity retention of 90.3% at 2.0 A and prominent cycling stability at 5.0 A g(-1) with the discharge capacity of 1210.1 mAh g(-1) after 400 cycles. When assembled to a full cell with commercial LiFePO4 as cathode, the full cell represents 360.7 mAh g(-1) after 30 cycles (based on the anode), which displays a development potential for practical application.
引用
收藏
页码:139 / 146
页数:15
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